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赋予大麦(Hordeum vulgare ssp. vulgare L.)对大麦黄花叶病毒复合体(BaMMV、BaYMV、BaYMV-2)抗性的Rym4/Rym5基因座的高分辨率定位。

High-resolution mapping of the Rym4/Rym5 locus conferring resistance to the barley yellow mosaic virus complex (BaMMV, BaYMV, BaYMV-2) in barley (Hordeum vulgare ssp. vulgare L.).

作者信息

Pellio Bettina, Streng Stefan, Bauer Eva, Stein Nils, Perovic Dragan, Schiemann Andrea, Friedt Wolfgang, Ordon Frank, Graner Andreas

机构信息

Institute of Crop Science and Plant Breeding I, Justus-Liebig-University, Heinrich-Buff-Ring 26-32, 35392, Giessen, Germany.

出版信息

Theor Appl Genet. 2005 Jan;110(2):283-93. doi: 10.1007/s00122-004-1832-4. Epub 2004 Nov 18.

Abstract

Soil-borne barley yellow mosaic virus disease--caused by a complex of at least three viruses, i.e. Barley mild mosaic virus (BaMMV), Barley yellow mosaic virus (BaYMV) and BaYMV-2--is one of the most important diseases of winter barley in Europe. The two genes rym4, effective against BaMMV and BaYMV, and rym5, additionally effective against BaYMV-2, comprise a complex locus on chromosome 3HL, which is of special importance to European barley breeding. To provide the genetic basis for positional cloning of the Rym4/Rym5 locus, two high-resolution maps were constructed based on co-dominant flanking markers (MWG838/Y57c10 - MWG010/Bmac29). Mapping at a resolution of about 0.05% rec., rym4 has been located 1.07% recombination distal of marker MWG838 and 1.21% recombination proximal to marker MWG010. Based on a population size of 3,884 F2 plants (0.013% recombination) the interval harbouring rym5 was delimited to 1.49+/-0.14% recombination. By testing segmental recombinant inbred lines (RILs) for reaction to the different viruses at a resolution of 0.05% rec. (rym4) and 0.019% rec. (rym5), no segregation concerning the reaction to the different viruses could be observed. AFLP-based marker saturation for rym4, using 932 PstI+2/MseI+3 primer combinations only resulted in three markers with the closest one linked at 0.9% recombination to the gene. Two of these markers detected epialleles arising from the differential cytosine methylation of PstI sites. Regarding rym5, profiling of 1,200 RAPD primers (about 18,000 loci) and 2,048 EcoRI+3/MseI+3 AFLP primer combinations (about 205,000 loci) resulted in one RAPD marker and seven AFLP markers tightly linked to the resistance gene. Flanking markers with the closest linkage to rym5 (0.05% and 0.88% recombination) were converted into STS markers. These markers provide a starting point for chromosomal walking and may be exploited in marker-assisted selection for virus resistance based on rym5.

摘要

由至少三种病毒组成的复合病毒引起的土传大麦黄花叶病毒病,即大麦轻花叶病毒(BaMMV)、大麦黄花叶病毒(BaYMV)和BaYMV - 2,是欧洲冬大麦最重要的病害之一。两个对BaMMV和BaYMV有效的基因rym4以及另外对BaYMV - 2有效的基因rym5,在3HL染色体上构成一个复合位点,这对欧洲大麦育种具有特殊重要性。为了为Rym4/Rym5位点的定位克隆提供遗传基础,基于共显性侧翼标记(MWG838/Y57c10 - MWG010/Bmac29)构建了两个高分辨率图谱。以约0.05%重组率的分辨率进行定位,rym4位于标记MWG838的1.07%重组远端和标记MWG010的1.21%重组近端。基于3884个F2植株的群体规模(0.013%重组率),含有rym5的区间被限定为1.49±0.14%重组率。通过以0.05%重组率(rym4)和0.019%重组率(rym5)检测分段重组自交系(RILs)对不同病毒的反应,未观察到对不同病毒反应的分离现象。仅使用932种PstI + 2/MseI + 3引物组合对rym4进行基于AFLP的标记饱和分析,仅产生了三个标记,其中与该基因连锁最紧密的一个位于0.9%重组率处。这些标记中的两个检测到了由PstI位点的差异胞嘧啶甲基化产生的表观等位基因。关于rym5,对1200个RAPD引物(约18000个位点)和2048种EcoRI + 3/MseI + 3 AFLP引物组合(约205000个位点)进行分析,得到了一个与抗性基因紧密连锁的RAPD标记和七个AFLP标记。与rym5连锁最紧密的侧翼标记(0.05%和0.88%重组率)被转化为STS标记。这些标记为染色体步移提供了起点,可用于基于rym5的病毒抗性标记辅助选择。

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